scholarly journals Mitochondrial DNA variation and the evolution of Robertsonian chromosomal races of house mice, Mus domesticus.

Genetics ◽  
1994 ◽  
Vol 136 (3) ◽  
pp. 1105-1120 ◽  
Author(s):  
M W Nachman ◽  
S N Boyer ◽  
J B Searle ◽  
C F Aquadro

Abstract The house mouse, Mus domesticus, includes many distinct Robertsonian (Rb) chromosomal races with diploid numbers from 2n = 22 to 2n = 38. Although these races are highly differentiated karyotypically, they are otherwise indistinguishable from standard karyotype (i.e., 2n = 40) mice, and consequently their evolutionary histories are not well understood. We have examined mitochondrial DNA (mtDNA) sequence variation from the control region and the ND3 gene region among 56 M. domesticus from Western Europe, including 15 Rb populations and 13 standard karyotype populations, and two individuals of the sister species, Mus musculus. mtDNA exhibited an average sequence divergence of 0.84% within M. domesticus and 3.4% between M. domesticus and M. musculus. The transition/transversion bias for the regions sequenced is 5.7:1, and the overall rate of sequence evolution is approximately 10% divergence per million years. The amount of mtDNA variation was as great among different Rb races as among different populations of standard karyotype mice, suggesting that different Rb races do not derive from a single recent maternal lineage. Phylogenetic analysis of the mtDNA sequences resulted in a parsimony tree which contained six major clades. Each of these clades contained both Rb and standard karyotype mice, consistent with the hypothesis that Rb races have arisen independently multiple times. Discordance between phylogeny and geography was attributable to ancestral polymorphism as a consequence of the recent colonization of Western Europe by mice. Two major mtDNA lineages were geographically localized and contained both Rb and standard karyotype mice. The age of these lineages suggests that mice have moved into Europe only within the last 10,000 years and that Rb populations in different geographic regions arose during this time.

1993 ◽  
Vol 50 (10) ◽  
pp. 2112-2118 ◽  
Author(s):  
S. Fournier Lockwood ◽  
Robert E. Dillinger Jr. ◽  
Tim P. Birt ◽  
John M. Green ◽  
Thomas P. Snyder

We determined the DNA sequence of a portion of the mitochondrial cytochrome b gene for eight members of the Coregoninae (Salmonidae) from North America in an effort to elucidate phylogenetic relationships in the subfamily. DNA was prepared for sequencing by the polymerase chain reaction (PCR). Direct estimates of mitochondrial DNA (mtDNA) sequence divergence among taxa ranged from 0.0% between Arctic cisco (Coregonus autumnalis) from the Mackenzie River, Canada, and cisco (C. artedi) from the Laurentian Great Lakes to 5.8% between the inconnu (Stenodus leucichthys) and the round whitefish (Prosopium cylindraceum). As has been noted in other fish species and vertebrates in general, third position silent substitutions predominated over any other type of nucleotide change. No amino acid replacement substitutions were found among any of the eight taxa examined. Comparison of mtDNA sequence divergence estimates from this and other studies suggests that the radiation of the genera within the Coregoninae occurred relatively recently (2–6 million yr B.P.). Cladistic analysis of the mtDNA sequence data yields a hypothesis of relationships that supports previous genetic and morphological classifications of coregonines.


1992 ◽  
Vol 337 (1280) ◽  
pp. 167-175 ◽  

The most critical and controversial feature of the African origin hypothesis of human mitochondrial DNA (mtDNA) evolution is the relatively recent age of about 200 ka inferred for the human mtDNA ancestor. If this age is wrong, and the actual age instead approaches 1 million years ago, then the controversy abates. Reliable estimates of the age of the human mtDNA ancestor and the associated standard error are therefore crucial. However, more recent estimates of the age of the human ancestor rely on comparisons between human and chimpanzee mtDNAs that may not be reliable and for which standard errors are difficult to calculate. We present here two approaches for deriving an intraspecific calibration of the rate of human mtDNA sequence evolution that allow standard errors to be readily calculated. The estimates resulting from these two approaches for the age of the human mtDNA ancestor (and approximate 95% confidence intervals) are 133 (63-356) and 137 (63-416) ka ago. These results provide the strongest evidence yet for a relatively recent origin of the human mtDNA ancestor.


1997 ◽  
Vol 24 (3) ◽  
pp. 289 ◽  
Author(s):  
M. D. B. Eldridge

The extent of mitochondrial DNA divergence between populations of the vulnerable yellow-footed rock- wallaby, Petrogale xanthopus, was assessed by restriction analysis. Of the 15 restriction endonucleases, five were informative, with a single unique haplotype identified in P. x. celeris from Queensland (Qld) (n = 8) and a further two unique haplotypes in three sampled populations of P. x. xanthopus from New South Wales (NSW) (n = 1) and South Australia (SA) (n = 9). The two subspecies of P. xanthopus were found to be genetically distinct (average sequence divergence = 0·72%). As this divergence is greater than that found between some Petrogale species, it is recommended that populations of P. x. xanthopus and P. x. celeris be managed independently both in captivity and the wild. The NSW population of P. x. xanthopus appears genetically similar to those in SA, although these data are limited.


1989 ◽  
Vol 67 (4) ◽  
pp. 891-907 ◽  
Author(s):  
Isaac I. Wirgin ◽  
Rui Proenca ◽  
Joseph Grossfield

Mitochondrial DNA (mtDNA) genotypes were determined for Atlantic striped bass from the St. Johns River in northeastern Florida and several hatchery reared individuals from Monck's Corner, South Carolina. Adults and hatchery-reared descendants of striped bass with high lateral line scale counts were sampled from several sites in the Apalachicola River system along the Gulf coast of Florida. In addition, naturally reproduced 1985 year class juveniles from the Apalachicola system were sampled. All mtDNA genotypes were compared with those observed in our sample of approximately 200 fish from the Atlantic coastal migratory stock. Ten different restriction endonucleases were used, generating 169 mtDNA fragments in most individuals. Heteroplasmy was observed in striped bass from both the St. Johns River and the Apalachicola system. Base sequence divergence among the populations surveyed was extremely low (maximum p = 0.0004), among the lowest reported for any animal species to date. However, the restriction enzymes RsaI and XbaI both revealed base substitutions unique to populations of Gulf Coast striped bass. Approximately 57% of striped bass from the Apalachicola system displayed an XbaI genotype not seen in any of our Atlantic collections. Four discrete mtDNA size classes were detected, differing by approximately 200, 300, and 400 base pairs from the smallest mtDNA molecule observed. The largest genotype was only seen in the Apalachicola system. The smallest genotype, while restricted to Gulf Coast striped bass sampled for this study, has been frequently observed in the Atlantic coastal migratory stock. The presence of mtDNA genotypes unique to the Apalachicola systems suggests the continued existence of a maternal lineage of striped bass of Gulf ancestry and points to the use of mtDNA as a valuable tag in the management of these populations. The lack of mtDNA sequence divergence in striped bass suggests a very recent origin for these populations.


Genes ◽  
2021 ◽  
Vol 12 (2) ◽  
pp. 155
Author(s):  
Kefena Effa ◽  
Sonia Rosenbom ◽  
Jianlin Han ◽  
Tadelle Dessie ◽  
Albano Beja-Pereira

Matrilineal genetic diversity and relationship were investigated among eight morphologically identified native Ethiopian horse populations using polymorphisms in 46 mtDNA D-loop sequences (454 base pairs). The horse populations identified were Abyssinian, Bale, Borana, Horro, Kafa, Kundido feral horses, Ogaden and Selale. Mitochondrial DNA D-loop sequences were characterized by 15 variable sites that defined five different haplotypes. All genetic diversity estimates, including Reynolds’ linearized genetic distance, genetic differentiation (FST) and nucleotide sequence divergence (DA), revealed a low genetic differentiation in native Ethiopian horse populations. However, Kundido feral and Borana domestic horses were slightly diverged from the rest of the Ethiopian horse populations. We also tried to shed some light on the matrilineal genetic root of native Ethiopian horses from a network constructed by combining newly generated haplotypes and reference haplotypes deposited in the GenBank for Eurasian type Turkish Anatolian horses that were used as a genetic conduit between Eurasian and African horse populations. Ninety-two haplotypes were generated from the combined Ethio-Eurasian mtDNA D-loop sequences. A network reconstructed from the combined haplotypes using Median-Joining algorithm showed that haplotypes generated from native Ethiopian horses formed separate clusters. The present result encourages further investigation of the genetic origin of native African horses by retrieving additional mtDNA sequences deposited in the GenBank for African and Eurasian type horses.


2018 ◽  
Vol 19 (12) ◽  
pp. 4039 ◽  
Author(s):  
Mi-Li Liu ◽  
Wei-Bing Fan ◽  
Ning Wang ◽  
Peng-Bin Dong ◽  
Ting-Ting Zhang ◽  
...  

Plant plastomes play crucial roles in species evolution and phylogenetic reconstruction studies due to being maternally inherited and due to the moderate evolutionary rate of genomes. However, patterns of sequence divergence and molecular evolution of the plastid genomes in the horticulturally- and economically-important Lonicera L. species are poorly understood. In this study, we collected the complete plastomes of seven Lonicera species and determined the various repeat sequence variations and protein sequence evolution by comparative genomic analysis. A total of 498 repeats were identified in plastid genomes, which included tandem (130), dispersed (277), and palindromic (91) types of repeat variations. Simple sequence repeat (SSR) elements analysis indicated the enriched SSRs in seven genomes to be mononucleotides, followed by tetra-nucleotides, dinucleotides, tri-nucleotides, hex-nucleotides, and penta-nucleotides. We identified 18 divergence hotspot regions (rps15, rps16, rps18, rpl23, psaJ, infA, ycf1, trnN-GUU-ndhF, rpoC2-rpoC1, rbcL-psaI, trnI-CAU-ycf2, psbZ-trnG-UCC, trnK-UUU-rps16, infA-rps8, rpl14-rpl16, trnV-GAC-rrn16, trnL-UAA intron, and rps12-clpP) that could be used as the potential molecular genetic markers for the further study of population genetics and phylogenetic evolution of Lonicera species. We found that a large number of repeat sequences were distributed in the divergence hotspots of plastid genomes. Interestingly, 16 genes were determined under positive selection, which included four genes for the subunits of ribosome proteins (rps7, rpl2, rpl16, and rpl22), three genes for the subunits of photosystem proteins (psaJ, psbC, and ycf4), three NADH oxidoreductase genes (ndhB, ndhH, and ndhK), two subunits of ATP genes (atpA and atpB), and four other genes (infA, rbcL, ycf1, and ycf2). Phylogenetic analysis based on the whole plastome demonstrated that the seven Lonicera species form a highly-supported monophyletic clade. The availability of these plastid genomes provides important genetic information for further species identification and biological research on Lonicera.


1982 ◽  
Vol 40 (1) ◽  
pp. 41-57 ◽  
Author(s):  
Robert W. Chapman ◽  
J. Claiborne Stephens ◽  
Robert A. Lansman ◽  
John C. Avise

SUMMARYThe future value of mitochondrial DNA (mtDNA) sequence information to studies in population biology will depend in part on understanding of mtDNA transmission genetics both within cell lineages and between animal generations. A series of stochastic models has been constructed here based on various possibilities concerning this transmission. Several of the models generate predictions inconsistent with available data and, hence, their assumptions are provisionally rejected. Other models cannot yet be falsified. These latter models include assumptions that (1) mtDNA's are sorted through cellular lineages by random allocation to daughter cells in germ cell lineages; (2) the effective intracellular population sizes (nM's) of mtDNA's are small; and (3) sperm may (or may not) provide a low level ‘gene-flow’ bridge between otherwise isolated female lineages. It is hoped that the models have helped to identify and will stimulate further empirical study of various parameters likely to strongly influence mtDNA evolution. In particular, critical experiments or measurements are needed to determine the effective sizes of mtDNA populations in germ (and somatic) cells and to examine possible paternal contributions to zygote mtDNA composition.


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